Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome (Q34015390)
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Current Data About Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome
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(P1476) "Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome" (language: en)
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A Lucassen
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J R W Yates
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J Clayton-Smith
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H Ilyina
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S Christin-Maitre
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M Fellous
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J P Fryns
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J R Kim
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P Lapunzina
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E Lemyre
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L M Messiaen
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C Oley
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